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What is the best treatment target in axial spondyloarthritis: tumour necrosis factor α, interleukin 17, or both?

Denis Poddubnyy1,2, Joachim Sieper1

  • 1Department of Gastroenterology, Infectiology and Rheumatology, Campus Benjamin Franklin, Charité Universitätsmedizin Berlin, Germany.

Insights

Tumor necrosis factor (TNF) blockers and interleukin-17 (IL-17) inhibitors show similar efficacy in treating axial spondyloarthritis. This finding opens new avenues for optimizing treatment strategies and understanding disease pathogenesis.

Area of Science:

  • Rheumatology
  • Immunology
  • Pharmacology

Background:

  • Tumor necrosis factor (TNF) inhibitors have been the primary targeted therapy for axial spondyloarthritis (axSpA) refractory to conventional treatments for over 15 years.
  • The emergence of interleukin-17 (IL-17) inhibitors provides a new therapeutic option for these patients.

Purpose of the Study:

  • To compare the efficacy of IL-17 inhibitors with established TNF blockers in axial spondyloarthritis.
  • To explore the implications of these findings for disease pathogenesis and future treatment strategies.

Main Methods:

  • Indirect comparison of treatment effects between TNF inhibitors and IL-17 inhibitors based on existing clinical trial data.
  • Review and discussion of current understanding of axSpA pathogenesis.

Main Results:

  • IL-17 inhibition demonstrates comparable efficacy to TNF blockers in axial spondyloarthritis patients.
  • Efficacy appears to be on a similar level between the two drug classes through indirect comparisons.

Conclusions:

  • IL-17 inhibitors represent a significant advancement in treating axial spondyloarthritis, offering an alternative to TNF blockers.
  • Further research is needed to address key questions regarding pathogenesis and to optimize therapeutic approaches for axSpA.

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